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化驗
99.95%
形狀
wire
製造商／商標名
Goodfellow 077-126-70
電阻係數
81 μΩ-cm, 20°C
長度 × 直徑
100 mm × 1.0 mm
bp
1527 °C (lit.)
mp
822 °C (lit.)
密度
5.24 g/mL at 25 °C (lit.)
SMILES 字串
[Eu]
InChI
1S/Eu
InChI 密鑰
OGPBJKLSAFTDLK-UHFFFAOYSA-N
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一般說明
For updated SDS information please visit www.goodfellow.com.
法律資訊
Product of Goodfellow
Satoshi Sakamoto et al.
Clinical chemistry, 60(4), 610-620 (2014-01-18)
Accurate detection and monitoring of disease-related biomarkers is important in understanding pathophysiology. We devised a rapid immunoreaction system that uses submicrometer polymer-coated fluorescent ferrite (FF) beads containing both ferrites (magnetic iron oxide) and fluorescent europium complexes. FF beads were prepared
A S L Caldwell et al.
Endocrinology, 156(4), 1441-1452 (2015-02-03)
Polycystic ovary syndrome (PCOS) is associated with reproductive, endocrine, and metabolic abnormalities. Because hyperandrogenism is the most consistent PCOS feature, we used wild-type (WT) and androgen receptor (AR) knockout (ARKO) mice, together with a mouse model of PCOS, to investigate
M L P Reddy et al.
Dalton transactions (Cambridge, England : 2003), 42(43), 15249-15262 (2013-10-01)
Visible-light sensitized luminescent europium(III) molecular materials are of considerable importance because their outstanding photophysical properties make them well suited as labels in fluorescence-based bioassays and low-voltage driven pure red-emitters in optoelectronic technology. One challenge in this field is development of
Soo-Kyung Kim et al.
ChemMedChem, 9(8), 1732-1743 (2014-07-06)
Human Urotensin-II (U-II) is the most potent mammalian vasoconstrictor known.1 Thus, a U-II antagonist would be of therapeutic value in a number of cardiovascular disorders.2 Here, we describe our work on the prediction of the structure of the human U-II
Tsung-Sheng Wu et al.
Molecular endocrinology (Baltimore, Md.), 28(7), 1026-1038 (2014-06-04)
SHBG transports and regulates the activities of androgens and estrogens. Several single nucleotide polymorphisms in the human SHBG gene have been linked to sex steroid-dependent diseases, including those associated with the metabolic syndrome. The N-terminal laminin G-like domain of SHBG
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